Canonical Allele Identifier: CA376437873

Gene: MAP3K8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30450348T>C , CM000672.2:g.30450348T>C	GRCh38
NC_000010.10:g.30739277T>C , CM000672.1:g.30739277T>C	GRCh37
NC_000010.9:g.30779283T>C	NCBI36
NG_029984.1:g.21328T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263056.6:c.595T>C MANE Select	ENSP00000263056.1:p.Trp199Arg
ENST00000263056.5:c.595T>C	ENSP00000263056.1:p.Trp199Arg
ENST00000375321.1:c.595T>C	ENSP00000364470.1:p.Trp199Arg
ENST00000413724.5:c.595T>C	ENSP00000391275.1:p.Trp199Arg
ENST00000415139.5:c.595T>C	ENSP00000409653.1:p.Trp199Arg
ENST00000430603.1:n.357T>C
ENST00000542547.5:c.595T>C	ENSP00000443610.1:p.Trp199Arg
NM_001244134.1:c.595T>C	NP_001231063.1:p.Trp199Arg
NM_005204.3:c.595T>C	NP_005195.2:p.Trp199Arg
XM_005252364.2:c.595T>C	XP_005252421.2:p.Trp199Arg
XM_011519308.1:c.976T>C	XP_011517610.1:p.Trp326Arg
XM_011519309.1:c.682T>C	XP_011517611.1:p.Trp228Arg
XM_011519310.1:c.661T>C	XP_011517612.1:p.Trp221Arg
XM_011519311.1:c.661T>C	XP_011517613.1:p.Trp221Arg
XM_011519312.1:c.661T>C	XP_011517614.1:p.Trp221Arg
XM_011519313.1:c.661T>C	XP_011517615.1:p.Trp221Arg
XM_011519314.1:c.661T>C	XP_011517616.1:p.Trp221Arg
XM_011519315.1:c.661T>C	XP_011517617.1:p.Trp221Arg
NM_001320961.1:c.595T>C	NP_001307890.1:p.Trp199Arg
XM_017015708.1:c.595T>C	XP_016871197.1:p.Trp199Arg
XM_017015709.2:c.595T>C	XP_016871198.1:p.Trp199Arg
XM_017015710.1:c.595T>C	XP_016871199.1:p.Trp199Arg
XM_017015711.2:c.106T>C	XP_016871200.1:p.Trp36Arg
XM_017015712.1:c.106T>C	XP_016871201.1:p.Trp36Arg
XM_017015713.1:c.106T>C	XP_016871202.1:p.Trp36Arg
XM_017015714.1:c.106T>C	XP_016871203.1:p.Trp36Arg
XM_024447819.1:c.106T>C	XP_024303587.1:p.Trp36Arg
NM_005204.4:c.595T>C MANE Select	NP_005195.2:p.Trp199Arg
NM_001320961.2:c.595T>C	NP_001307890.1:p.Trp199Arg